نتایج جستجو برای: carbonyl compound

تعداد نتایج: 139449  

2016
John-Michael Collinson James D. E. T. Wilton-Ely Silvia Díez-González

A novel NHC–palladium(II) (NHC = N-heterocyclic carbene) complex and its immobilised version have been prepared and fully characterised. Optimisation studies led to good catalytic activities in Suzuki-Miyaura cross coupling and chloroarene dehalogenation reactions. Furthermore, the unexpected palladium-mediated transfer hydrogenation of a carbonyl compound is reported.

2012
Urmila Berar

Chalcones are a class of α,β-unsaturated carbonyl compounds that form the central core for a variety of naturally occurring biologically active compounds. They exhibit tremendous potential to act as a pharmacological agent. Besides their various pharmacological activities, chalcones have been explored for different optical applications including second harmonic generation materials in non-linea...

2015
Marcin Kalek Gregory C. Fu

Methods have recently been developed for the phosphine-catalyzed asymmetric γ-addition of nucleophiles to readily available allenoates and alkynoates to generate useful α,β-unsaturated carbonyl compounds that bear a stereogenic center in either the γ or the δ position (but not both) with high stereoselectivity. The utility of this approach would be enhanced considerably if the stereochemistry a...

Journal: :The Journal of chemical physics 2008
Marko Schreiber Mario R Silva-Junior Stephan P A Sauer Walter Thiel

A benchmark set of 28 medium-sized organic molecules is assembled that covers the most important classes of chromophores including polyenes and other unsaturated aliphatic compounds, aromatic hydrocarbons, heterocycles, carbonyl compounds, and nucleobases. Vertical excitation energies and one-electron properties are computed for the valence excited states of these molecules using both multiconf...

Journal: :Dalton transactions 2009
Xuanhua Chen Wenli Jia Rongwei Guo Todd W Graham Meredith A Gullons Kamaluddin Abdur-Rashid

The pressure hydrogenation capabilities of the iridium pincer complexes IrH2Cl[((i)Pr2PC2H4)2NH] (1) and IrH3[((i)Pr2PC2H4)2NH] (2) are described and compared to related results obtained previously in transfer hydrogenation. Complex 1 was shown to act as a convenient air-stable entry point to the active catalyst 2, in the presence of base and hydrogen gas. The catalysts are active in a range of...

Journal: :Dalton transactions 2015
Davud Karimian Bahram Yadollahi Valiollah Mirkhani

Herein, the synthesis, characterization and photocatalytic application of a novel hybrid polyoxometalate, which can absorb light in the visible region, are reported. This hybrid material was synthesized by attaching a monovacant polyoxometalate, (SiW11O39), through a (3-aminopropyl)triethoxysilane linker to the anthracene. The hybridization with anthracene drastically decreased the band gap of ...

2017
Andrea Porcheddu Evelina Colacino Giancarlo Cravotto Francesco Delogu Lidia De Luca

The present work addresses the development of an eco-friendly and cost-efficient protocol for the oxidation of primary and secondary alcohols to the corresponding aldehydes and ketones by mechanical processing under air. Ball milling was shown to promote the quantitative conversion of a broad set of alcohols into carbonyl compounds with no trace of an over-oxidation to carboxylic acids. The mec...

2003
Nagatoshi Nishiwaki Mina Tamura Kazushige Hori Yasuo Tohda Masahiro Ariga

3-Methyl-5-nitropyrimidin-4(3H)-one readily reacts with carbonyl compounds to produce three kinds of ring transformations. The nitropyrimidinone behaves as the synthetic equivalent of activated diformylamine affording 3,5-difunctionalized 4-pyridones, 4,5disubstituted pyrimidines and functionalized 4-aminopyridines. It also behaves like α-nitroformylacetic acid to give 5,6-disubstituted 3-nitro...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Riccardo Sinisi Jianwei Sun Gregory C Fu

Because carbonyl groups are ubiquitous in organic chemistry, the ability to synthesize functionalized carbonyl compounds, particularly enantioselectively, is an important objective. We have developed a straightforward and versatile method for catalytic asymmetric carbon-carbon bond formation at the γ-position of carbonyl compounds, specifically, phosphine-catalyzed additions of malonate esters ...

2008

When the hydrate reverts to starting materials, either of its two oxygen atoms must leave: one came from the water and one from the carbonyl group, so 50% of the time the oxygen atom that belonged to the carbonyl group will be lost. Usually, this is of no consequence, but it can be useful. For example, in 1968 some chemists studying the reactions that take place inside mass spectrometers needed...

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